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Testosterone therapy improved symptoms in a woman with congenital adrenal hyperplasia.

A truncated protein linked to breast cancer may change cell adhesion.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

TRH stimulates human hair growth and extends the hair growth phase.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

CCCA may be caused by both hair traction and an immune response.

A unique type of complex cyst was found on a man's scrotum.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

MCTD should be considered in children with recurring muscle issues, lupus-like symptoms, and edema.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Hair cortisol content can indicate cortisol exposure and varies with age, puberty, and BMI in youth.

A woman developed severe bladder inflammation after cancer treatment with Cytoxan.

Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Hair casts are harmless but can be mistaken for head lice.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

Trichoscopic examination is crucial for diagnosing congenital triangular alopecia.

HLD10 can include increased body hair and Mongolian spots.